A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102259



Internal ID22011495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8202576..8202576hg38UCSC Ensembl
chrUn_gl000220:102077..102077hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102259
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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